| Literature DB >> 30558885 |
Sawako Yamashiro1, Daisuke Taniguchi2, Soichiro Tanaka3, Tai Kiuchi2, Dimitrios Vavylonis4, Naoki Watanabe5.
Abstract
Fluorescent markers that bind endogenous target proteins are frequently employed for quantitative live-cell imaging. To visualize the actin cytoskeleton in live cells, several actin-binding probes have been widely used. Among them, Lifeact is the most popular probe with ideal properties, including fast exchangeable binding kinetics. Because of its fast kinetics, Lifeact is generally believed to distribute evenly throughout cellular actin structures. In this study, however, we demonstrate misdistribution of Lifeact toward the rear of lamellipodia where actin filaments continuously move inward along the retrograde flow. Similarly, phalloidin showed biased misdistribution toward the rear of lamellipodia in live cells. We show evidence of convection-induced misdistribution of actin probes by both experimental data and physical models. Our findings warn about the potential error arising from the use of target-binding probes in quantitative live imaging.Entities:
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Year: 2018 PMID: 30558885 PMCID: PMC6342703 DOI: 10.1016/j.bpj.2018.11.022
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033